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Clinical Trial Summary

The purpose of this clinical study is to collect performance and safety data for post-market Medtronic devices indicated for cranial and/or spinal indication(s). Subjects are enrolled and followed postoperatively for up to 24 months. The Ailliance clinical study is intended to collect data congruous with routine clinical care practices.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05856370
Study type Interventional
Source Medtronic Spinal and Biologics
Contact Katelynn Hamer
Phone 630-544-9247
Email katelynn.m.hamer@medtronic.com
Status Recruiting
Phase N/A
Start date May 1, 2023
Completion date April 2027

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